Welcome to LookChem.com Sign In|Join Free
  • or
6-Methoxy-5-(trifluoromethyl)pyridin-2-amine is a pyridine derivative with the molecular formula C7H8F3NO. It features a methoxy group and a trifluoromethyl substituent on the 5th and 2nd carbon atoms, respectively. This chemical compound serves as a versatile intermediate in the synthesis of various biologically active molecules and crop protection agents.

405160-57-8

Post Buying Request

405160-57-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

405160-57-8 Usage

Uses

Used in Pharmaceutical Industry:
6-Methoxy-5-(trifluoroMethyl)pyridin-2-aMine is used as a building block for the synthesis of pharmaceuticals. It contributes to the development of biologically active molecules that can be utilized in the creation of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 6-Methoxy-5-(trifluoroMethyl)pyridin-2-aMine is employed as a key component in the production of crop protection agents. Its role in the synthesis of these agents helps to ensure the development of effective solutions for agricultural pest control and crop enhancement.
Used in Research and Development for Medicinal Chemistry:
6-Methoxy-5-(trifluoroMethyl)pyridin-2-amine is utilized in research and development for medicinal chemistry, where it serves as an important intermediate in drug discovery. Its unique structure allows for the exploration of new chemical entities with potential therapeutic applications.
Used in Research and Development for Drug Discovery:
6-Methoxy-5-(trifluoroMethyl)pyridin-2-aMine is also used in drug discovery research, where it plays a crucial role in the synthesis and development of new pharmaceutical agents. Its presence in the molecular structure can influence the pharmacological properties of the resulting compounds, making it a valuable asset in the search for novel treatments.
Overall, 6-Methoxy-5-(trifluoroMethyl)pyridin-2-aMine is a significant intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals, playing a vital role in the advancement of various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 405160-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,5,1,6 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 405160-57:
(8*4)+(7*0)+(6*5)+(5*1)+(4*6)+(3*0)+(2*5)+(1*7)=108
108 % 10 = 8
So 405160-57-8 is a valid CAS Registry Number.

405160-57-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-2-methoxy-3-trifluoromethylpyridine

1.2 Other means of identification

Product number -
Other names 6-methoxy-5-(trifluoromethyl)pyridin-2-amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:405160-57-8 SDS

405160-57-8Relevant academic research and scientific papers

A practical preparation of methyl 2-methoxy-6-methylaminopyridine-3-carboxylate from 2,6-dichloro-3-trifluoromethylpyridine

Horikawa,Hirokawa,Kato

, p. 1621 - 1627 (2007/10/03)

An effective and practical synthetic route to methyl 2-methoxy-6-methylaminopyridine-3-carboxylate (7), the key intermediate of 5-bromo-2-methoxy-6-methylaminopyridine-3-carboxylic acid (1), from 2,6-dichloro-3-trifluoromethylpyridine (12) was undertaken. Process improvements were highlighted by regioselectivity of 12 with a nitrogen nucleophile and conversion of the 3- trifluoromethyl group into the methoxycarbonyl group. The reaction of 12 with N-benzylmethylamine provided the 6-(N-benzyl-N-methyl)aminopyridine 26a and the regioisomer 26b in >98: 2 ratio in a quantitative yield. Treatment of 2-methoxy-6-methylamino-3-trifluoropyridine (14a) with a large excess of sodium methoxide followed by acid hydrolysis gave the pyridine-3-carboxylic ester 7 in an excellent yield. The potential application of this reaction is also described.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 405160-57-8